Ki-67/CD3 ratio in the diagnosis of chronic inflammatory enteropathy in dogs.


Journal

Journal of veterinary internal medicine
ISSN: 1939-1676
Titre abrégé: J Vet Intern Med
Pays: United States
ID NLM: 8708660

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 16 05 2019
accepted: 26 11 2019
pubmed: 12 12 2019
medline: 22 10 2020
entrez: 12 12 2019
Statut: ppublish

Résumé

T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker for T cells. In human medicine, Ki-67 is an indicator for cell growth but there are only a few studies in dogs with CIE. To investigate Ki-67 in relation to T cells as a marker for CIE in dogs. Eleven dogs with CIE and 6 healthy beagle controls (CO). Retrospective case-control study. Dogs were clinically assessed by the Canine Chronic Enteropathy Clinical Activity Index (CCECAI). Duodenal mucosal biopsy samples were endoscopically obtained for histopathologic examination by means of the World Small Animal Veterinary Association score. Double-labeled immunofluorescence was used to investigate colocalization of Ki-67 and CD3 in epithelium and lamina propria (LP) of villi and crypts. Dogs with CIE had significantly higher clinical score (median, 5.0; interquartile range [IQR], 3-7) compared to CO (all 0; P < .001). The Ki-67/CD3 double-positive cells were significantly increased in the LP of the crypt region of CIE dogs (0.63 cells/mm The Ki-67/CD3 ratio is upregulated in the LP crypt region of dogs with CIE and it correlates with clinical severity. Therefore, Ki-67/CD3 could be a useful tool for detection of CIE.

Sections du résumé

BACKGROUND BACKGROUND
T cells play a key role in the pathogenesis of chronic inflammatory enteropathy (CIE) in dogs. Cluster of differentiation 3 (CD3) antigen serves as a marker for T cells. In human medicine, Ki-67 is an indicator for cell growth but there are only a few studies in dogs with CIE.
OBJECTIVE OBJECTIVE
To investigate Ki-67 in relation to T cells as a marker for CIE in dogs.
ANIMALS METHODS
Eleven dogs with CIE and 6 healthy beagle controls (CO).
METHODS METHODS
Retrospective case-control study. Dogs were clinically assessed by the Canine Chronic Enteropathy Clinical Activity Index (CCECAI). Duodenal mucosal biopsy samples were endoscopically obtained for histopathologic examination by means of the World Small Animal Veterinary Association score. Double-labeled immunofluorescence was used to investigate colocalization of Ki-67 and CD3 in epithelium and lamina propria (LP) of villi and crypts.
RESULTS RESULTS
Dogs with CIE had significantly higher clinical score (median, 5.0; interquartile range [IQR], 3-7) compared to CO (all 0; P < .001). The Ki-67/CD3 double-positive cells were significantly increased in the LP of the crypt region of CIE dogs (0.63 cells/mm
CONCLUSIONS AND CLINICAL IMPORTANCE CONCLUSIONS
The Ki-67/CD3 ratio is upregulated in the LP crypt region of dogs with CIE and it correlates with clinical severity. Therefore, Ki-67/CD3 could be a useful tool for detection of CIE.

Identifiants

pubmed: 31825538
doi: 10.1111/jvim.15680
pmc: PMC6979107
doi:

Substances chimiques

CD3 Complex 0
Ki-67 Antigen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

92-97

Informations de copyright

© 2019 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine.

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Auteurs

Sonja Karlovits (S)

Department for Companion Animals and Horses, Clinic for Small Animal Internal Medicine, University of Veterinary Medicine, Vienna, Austria.

Anita Manz (A)

Department for Companion Animals and Horses, Clinic for Small Animal Internal Medicine, University of Veterinary Medicine, Vienna, Austria.

Karin Allenspach (K)

Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Iowa State University, Ames, Iowa.

Ingrid Walter (I)

VetCore Facility for Research, University of Veterinary Medicine, Vienna, Austria.
Department for Pathobiology, Institute of Pathology, University of Veterinary Medicine, Vienna, Austria.

Stefan Kummer (S)

VetCore Facility for Research, University of Veterinary Medicine, Vienna, Austria.

Alexander Tichy (A)

Department of Biomedical Sciences, University of Veterinary Medicine, Vienna, Austria.

Barbara Richter (B)

Department for Pathobiology, Institute of Pathology, University of Veterinary Medicine, Vienna, Austria.

Iwan A Burgener (IA)

Department for Companion Animals and Horses, Clinic for Small Animal Internal Medicine, University of Veterinary Medicine, Vienna, Austria.

Nicole Luckschander-Zeller (N)

Department for Companion Animals and Horses, Clinic for Small Animal Internal Medicine, University of Veterinary Medicine, Vienna, Austria.

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Classifications MeSH